Variant (rsID / SNP)

rs115027760

rs115027760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEUROD1. Location: chromosome 2, position 182,542,811. Clinical significance in the table: Likely benign.

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Reference-table entries

NEUROD1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:182542811
Cytoband: 2q31.3
HGVS: NM_002500.5(NEUROD1):c.777C>T (p.Ser259=)
Allele change: Silent

Associated conditions / phenotypes

Maturity-onset diabetes of the young type 6

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.